Evidence map›Paper›PMID 41261115›Full record

ArticleNature communications2025

Clinical and genomic features of Lynch syndrome differ by tumor site and disease spectrum.

Shisen Li, Ningning Luo, Gaoxin Jin, Tiantian Han, Xiangyu Yin, Didi Guo, Xing Zhang, Zhaobang Tan

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Shisen Li *Department of Digestive Surgery, Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an, Shanxi, China.ORCID http://orcid.org/0000-0002-9734-2829
Ningning Luo *The Medical Department, Jiangsu Simcere Diagnostics Co., Ltd., Nanjing Simcere Medical Laboratory Science Co., Ltd., The State Key Laboratory of Neurology and Oncology Drug Development, Nanjing, Jiangsu, China.ORCID http://orcid.org/0000-0002-1991-1168
Gaoxin JinDepartment of Gastrointestinal Surgery, The People's Hospital of Jimo.Qingdao, Qingdao, Shandong, China.ORCID http://orcid.org/0009-0009-3954-7701
Tiantian HanThe Medical Department, Jiangsu Simcere Diagnostics Co., Ltd., Nanjing Simcere Medical Laboratory Science Co., Ltd., The State Key Laboratory of Neurology and Oncology Drug Development, Nanjing, Jiangsu, China.ORCID http://orcid.org/0009-0003-9516-7355
Xiangyu YinDepartment of Biological Sciences, Xi'an Jiaotong-Liverpool University, Suzhou, China.ORCID http://orcid.org/0009-0004-7204-4659
Didi GuoThe Medical Department, Jiangsu Simcere Diagnostics Co., Ltd., Nanjing Simcere Medical Laboratory Science Co., Ltd., The State Key Laboratory of Neurology and Oncology Drug Development, Nanjing, Jiangsu, China.ORCID http://orcid.org/0009-0009-2236-4896
Xing ZhangThe Medical Department, Jiangsu Simcere Diagnostics Co., Ltd., Nanjing Simcere Medical Laboratory Science Co., Ltd., The State Key Laboratory of Neurology and Oncology Drug Development, Nanjing, Jiangsu, China. xing.zhang@simceredx.com.
Zhaobang TanDepartment of Digestive Surgery, Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an, Shanxi, China. ausgstudy@163.com.ORCID http://orcid.org/0000-0003-0249-0579

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lynch Syndrome (LS) carriers occasionally develop central nervous system (CNS) malignancies or tumors in organs not traditionally linked to the syndrome. These tumors are poorly characterized in the literature, and there is no sufficient consensus on guidelines and management recommendations for these tumors. Here we study LS from the tumor perspective and profile 238 pan-cancer specimens from 228 genetically confirmed LS carriers. Tumors are stratified into CNS LS-related, non-CNS LS-related, and non-CNS LS-unrelated groups according to anatomic site and established LS tumor spectrum. Comparative analyses against TCGA reveal significant alterations in LS incidence within endometrial and hepatic cancers. Across the three groups, we reveal marked heterogeneity in germline pathogenic-variant distribution, age at diagnosis, somatic mutation landscapes, tumor mutational burden, and microsatellite-instability status. This site- and spectrum-based stratification of a large, pan-cancer LS cohort underscores the heterogeneity of the LS and provides a data-driven foundation for refining future disease management strategies.

Indexed as

Colorectal Neoplasms, Hereditary NonpolyposisAdultAgedEndometrial NeoplasmsFemaleGenomicsGerm-Line MutationHumansLiver NeoplasmsMaleMicrosatellite InstabilityMiddle AgedMutation

Identifiers

PMID41261115
PMCPMC12630928

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.